Results 71 to 80 of about 9,989 (122)
Behçet’s disease, also known as the oral–ocular–genital syndrome, is a chronic systemic vasculitis characterized by recurrent oral and genital ulcers as well as ocular manifestations such as uveitis and conjunctivitis.
Dou Yuan
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Behçet’s disease (BD) is a vasculitis that affects vessels of any size. It is more frequent along the ancient Silk Road, extending from the Far East to the Mediterranean basin.
Ümmüşen Kaya Akca, Yelda Bilginer
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Retinal thickness and microvascular alterations in the diagnosis of behcet's disease: a case-control study. [PDF]
Xing ZM +11 more
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Ocular Manifestations of Pediatric Behçet's Disease. [PDF]
Nouraeinejad A.
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Neuro-Behçet's Disease Presenting as Recurrent Demyelinating Illness. [PDF]
Abirami S, Sivakumar S, Kumar SV.
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Identification of ATP9A-NFATC2 gene fusion transcript in Behcet's disease, a subtype of uveitis. [PDF]
Haridas K +5 more
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Severe neuro-behçet's disease refractory: Radiologic improvement with tocilizumab. [PDF]
Benyarou K +3 more
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Acute necrotising pancreatitis in a patient with Behçet's disease. [PDF]
Albadi AA +5 more
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Juvenile Behçet's disease 2014-2024: multicenter study in Colombia. [PDF]
Zabala-Sepúlveda LM +7 more
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Behcet's disease in a patient with chronic myeloid leukemia. [PDF]
Singh D +3 more
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